drugset / Trial / NCT05030415

Ixekizumab in Adult Patients With Lichen Planus and Lichen Planopilaris

NCT05030415

Phase 0 Completed 9 enrolled University of New Mexico
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the safety and efficacy of ixekizumab in lichen planus and lichen planopilaris clinical response by Total Body Surface (TBS) determination, Investigator Global Assessment (IGA) Score, Lichen Planopilaris Activity Index (LPPAI), and Frontal Fibrosing Alopecia Severity Score (FFASS).

Timeline

Start
2021-08-12
Primary completion
2024-03-25
Completion
2024-03-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Ixekizumab Monoclonal antibody 80 mg Subcutaneous